Evidence map›Paper›PMID 34816630›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Nano-Enabled Reposition of Proton Pump Inhibitors for TLR Inhibition: Toward A New Targeted Nanotherapy for Acute Lung Injury.

Liya Sun, Yuan Liu, Xiali Liu, Rui Wang, Jiameng Gong, Aabida Saferali, Wei Gao, Aying Ma, Huiqiang Ma, Stuart E Turvey and 2 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

Liya SunSchool of Biomedical Engineering, The Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, Intensive Care Unit of the Second Hospital, Tianjin Medical University, No. 22 Qixiangtai Road, Heping District, Tianjin, 300070, China.
Yuan LiuSchool of Biomedical Engineering, The Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, Intensive Care Unit of the Second Hospital, Tianjin Medical University, No. 22 Qixiangtai Road, Heping District, Tianjin, 300070, China.
Xiali LiuDepartment of Pulmonary and Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, No. 650 Xinsongjiang Road, Shanghai, 201620, China.
Rui WangSchool of Biomedical Engineering, The Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, Intensive Care Unit of the Second Hospital, Tianjin Medical University, No. 22 Qixiangtai Road, Heping District, Tianjin, 300070, China.
Jiameng GongSchool of Biomedical Engineering, The Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, Intensive Care Unit of the Second Hospital, Tianjin Medical University, No. 22 Qixiangtai Road, Heping District, Tianjin, 300070, China.
Aabida SaferaliChanning Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, 181 Longwood Avenue, Boston, MA, 02115, USA.
Wei GaoDepartment of Pulmonary and Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, No. 650 Xinsongjiang Road, Shanghai, 201620, China.
Aying MaDepartment of Pulmonary and Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, No. 650 Xinsongjiang Road, Shanghai, 201620, China.
Huiqiang MaSchool of Biomedical Engineering, The Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, Intensive Care Unit of the Second Hospital, Tianjin Medical University, No. 22 Qixiangtai Road, Heping District, Tianjin, 300070, China.
Stuart E TurveyBC Children's Research Institute, University of British Columbia, 950 West 28th Avenue, Vancouver, BC V5Z 4H4, Canada.
Shan-Yu FungDepartment of Immunology, Key Laboratory of Immune Microenvironment and Disease (Ministry of Education), The Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, School of Basic Medical Science, Tianjin Medical University, No. 22 Qixiangtai Road, Heping District, Tianjin, 300070, China.
Hong YangSchool of Biomedical Engineering, The Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, Intensive Care Unit of the Second Hospital, Tianjin Medical University, No. 22 Qixiangtai Road, Heping District, Tianjin, 300070, China.ORCID 0000-0002-6707-8481
Second Hospital of Tianjin Medical University · CNShanghai Jiao Tong University · CNBrigham and Women's Hospital · USTianjin Medical University · CNUniversity of British Columbia · CA

Funding

National Natural Science Foundation of China 81770070National Natural Science Foundation of China 81971549Natural Science Foundation of Tianjin Municipal Science and Technology Commission 20JCYBJC00040Tianjin Research Innovation Project for Postgraduate Students for support 2020YJSB136
6 · The paper itself

Abstract

Toll-like receptor (TLR) activation in macrophages plays a critical role in the pathogenesis of acute lung injury (ALI). While TLR inhibition is a promising strategy to control the overwhelming inflammation in ALI, there still lacks effective TLR inhibitors for clinical uses to date. A unique class of peptide-coated gold nanoparticles (GNPs) is previously discovered, which effectively inhibited TLR signaling and protected mice from lipopolysaccharide (LPS)-induced ALI. To fast translate such a discovery into potential clinical applicable nanotherapeutics, herein an elegant strategy of "nano-enabled drug repurposing" with "nano-targeting" is introduced to empower the existing drugs for new uses. Combining transcriptome sequencing with Connectivity Map analysis, it is identified that the proton pump inhibitors (PPIs) share similar mechanisms of action to the discovered GNP-based TLR inhibitor. It is confirmed that PPIs (including omeprazole) do inhibit endosomal TLR signaling and inflammatory responses in macrophages and human peripheral blood mononuclear cells, and exhibits anti-inflammatory activity in an LPS-induced ALI mouse model. The omeprazole is then formulated into a nanoform with liposomes to enhance its macrophage targeting ability and the therapeutic efficacy in vivo. This research provides a new translational strategy of nano-enabled drug repurposing to translate bioactive nanoparticles into clinically used drugs and targeted nano-therapeutics for ALI.

Indexed as

Acute Lung InjuryAnimalsDisease Models, AnimalFemaleHumansMaleMetal NanoparticlesMiceMice, Inbred C57BLNanomedicineProton Pump InhibitorsToll-Like ReceptorsProton Pump InhibitorsToll-Like Receptorsacute lung injurybioactive nanoparticlesdrug repurposinginflammationmacrophagesproton pump inhibitorsToll-like receptors

Identifiers

PMID34816630
PMCPMC8787384
OpenAlexW3216854271

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.